Canonical Allele Identifier: PA125202
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15371
ClinVar RCV Id: RCV000016623 RCV001811164
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Asp80Tyr
CA125201
NM_000518.5:c.238G>T